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HomeDrugsU.S. FDA Active Pharmaceutical Ingredients (API)API Examples › U.S. FDA Regulations: Benazepril Hydrochloride

U.S. FDA Requirements: Benazepril Hydrochloride

Pharmaceutical / Drug Definition : Inhibits conversion of angiotensin I to angiotensin II, a vasoconstrictor that stimulates adrenal glands and promotes aldosterone secretion, thereby reducing sodium and water reabsorption and ultimately decreasing blood pressure. Decreased angiotensin also causes increased potassium level and fluid loss.

In the United States, Benazepril Hydrochloride is regulated by the U.S. Food and Drug Administration (FDA). FDA has specific requirements regarding the registration and listing of Benazepril Hydrochloride.

Registrar Corp assists Benazepril Hydrochloride companies with:

  • FDA Registration Benazepril Hydrochloride
  • FDA Listing Benazepril Hydrochloride
  • FDA Label Requirements and Exceptions Benazepril Hydrochloride
  • FDA Import Information Benazepril Hydrochloride
  • FDA Detentions Benazepril Hydrochloride (Benazepril Hydrochloride Entry Refusal)
  • General U.S. Food and Drug Administration Guidelines for:
       - Manufacturers Benazepril Hydrochloride (Benazepril Hydrochloride Suppliers)
       - Processors Benazepril Hydrochloride
       - Repackers Benazepril Hydrochloride
       - Relabelers Benazepril Hydrochloride
       - Exporters Benazepril Hydrochloride
       - Importers Benazepril Hydrochloride
For more information about Benazepril Hydrochloride, simply click below:

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U.S. FDA Regulations:

U.S. FDA Regulation: 21 C.F.R. Part 207

Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
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